Chemistry - A European Journal · 2007 · 58 citations · 45 references
Life SciencesBiochemistryBioengineeringBiophysical ChemistryNucleic Acid BiochemistryNucleic Acid ChemistryDna ChemistryDna NanotechnologyDna StructureFluorescence SpectroscopyMolecular NanotechnologyOligonucleotide ChemistryAqueous Reaction MediaFluorophore ChemistryGround StatesHydrophobic InteractionsNucleic Acid FluorescenceOrganic FluorophoresSolid-phase Dna SynthesisSolid-phase Oligonucleotide Synthesis
DNA-like fluorescent oligomers composed of alkynyl beta-D-ribofuranosides bearing pyrene, perylene, and anthracene as a fluorophore were synthesized by solid-phase DNA synthesis. The fluorescent oligomers possess the defined number and order of the fluorophores. In these oligomers, the adjacent fluorophores efficiently interact with each other by hydrophobic interactions in their electronic ground states in a face-to-face fashion. The predominant excimer emissions were observed from not only the homooligomers (pyrene-pyrene and perylene-perylene systems) but also the heterooligomers (pyrene-perylene, pyrene-anthracene, and perylene-anthracene systems) in aqueous media.
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